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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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GenTek ® Scanbody — 14 UDI-DI variants, MDR (Zfx GmbH)

MD Atlas
Zfx GmbH

Data from EUDAMED, last updated May 23, 2026

GenTek ® Scanbody

42518817-GT-D-Scanbody-D7

14 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class I

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Zfx GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42518817-GT-D-Scanbody-D7
Device name: GenTek ® Scanbody
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: Zfx GmbH
SRN: DE-MF-000018101
Country: Germany
Email: qm@zfx-dental.com
Phone: +49 81313324420

Variants by status

UDI-DI variants

14 UDI-DI variants

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Applied filters

basicUdiUlid01KP3CFD2QTEWHGE0EC53ECRNN

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

ZFX05Z-ZB-CE-3404251881769005
ZFX05Z-ZB-TA-4504251881769203
ZFX05Z-ZB-EX-4104251881769104
ZFX05Z-ZB-TSV-5704251881769265
ZFX05Z-ZB-EX-6004251881769142
ZFX05Z-ZB-EX-3404251881769081
ZFX05Z-ZB-TSV-4504251881769241
ZFX05Z-ZB-TSV-3504251881769227
ZFX05Z-ZB-EZ-2904251881769166
ZFX05Z-ZB-CE-5004251881769043
ZFX05Z-ZB-EX-5004251881769128
ZFX05Z-ZB-CE-6004251881769067
ZFX05Z-ZB-CE-4104251881769029
ZFX05Z-ZB-LP-4804251881769180